chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230214666	230214667	C	G	31	GENIC	possibly homozygous	59431427
2	230215978	230215979	G	A	3	GENIC	homozygous	59431428
2	230216744	230216745	T	TG	13	GENIC	homozygous	59431429
2	230221078	230221079	T	A	16	GENIC	homozygous	59431432
2	230221165	230221166	G	A	31	GENIC	possibly homozygous	59431433
2	230221863	230221864	G	A	10	GENIC	homozygous	59431434
2	230222051	230222052	G	A	11	GENIC	heterozygous	59431435
2	230224092	230224093	T	TA	2	GENIC	homozygous	59431442
2	230224372	230224373	T	G	8	GENIC	homozygous	59431443
2	230224814	230224815	G	T	10	GENIC	homozygous	59431444
2	230224955	230224960	AAAAA	-----	1	GENIC	homozygous	60594465
2	230225496	230225497	T	C	4	GENIC	homozygous	59431447
2	230225498	230225499	G	A	4	GENIC	homozygous	59431448
2	230226225	230226226	A	G	10	GENIC	possibly homozygous	59431449
2	230226753	230226754	G	A	27	GENIC	homozygous	59431450
2	230226910	230226911	T	C	7	GENIC	homozygous	59431451
2	230226911	230226912	A	C	7	GENIC	homozygous	59431452
2	230227807	230227808	C	T	19	GENIC	homozygous	59431453
2	230227885	230227886	A	ATTAAGTTTGGCAT	3	GENIC	homozygous	59431454
2	230228408	230228409	A	T	18	GENIC	possibly homozygous	59431457
2	230228840	230228841	A	C	17	GENIC	homozygous	59431458
2	230229354	230229355	C	T	26	GENIC	homozygous	59431459
2	230229393	230229394	A	G	26	GENIC	homozygous	59431460
2	230229503	230229504	C	T	15	GENIC	possibly homozygous	59431461
2	230229629	230229630	T	G	23	GENIC	possibly homozygous	59431462
2	230229792	230229793	A	G	25	GENIC	possibly homozygous	59431463
2	230229951	230229952	G	A	19	GENIC	homozygous	59431464
2	230229978	230229979	G	A	16	GENIC	homozygous	59431465
2	230231121	230231123	CA	--	2	GENIC	homozygous	59431466
2	230231204	230231216	AGAGAGAGAGAG	------------	2	GENIC	heterozygous	59431467
2	230231564	230231565	G	A	22	GENIC	homozygous	59431468
2	230233690	230233691	C	CTGG	10	GENIC	homozygous	59431469
2	230234666	230234667	A	AG	19	GENIC	possibly homozygous	59431473